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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2389269Erstellt: 26. Oktober 2026

Triethylamine → Tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2389269

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTrifluoroacetic anhydrideHCID 9845—
EduktTert-butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylateHCID 11244883—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylateHCID 67154775—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The tert-butyl 4-[2-(aminocarbonyl)-1-benzofuran-5-yl]piperazine-1-carboxylate (85 mg, 0.246 mmol) was dissolved in 5 mL of DCM and cooled to 0° C. under nitrogen. Triethylamine (0.075 mL, 0.541 mmol) was added, followed by trifluoroacetic anhydride (0.038 mL, 0.271 mmol). The reaction was stirred for 1 hour, then was diluted with additional 20 mL of DCM and washed with water (2×40 mL). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to afford tert-butyl 4-(2-cyano-1-benzofuran-5-yl)piperazine-1-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08273737B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-e1c2fb2a86d248208d1585cf22ab9967
Quellennotizuspto-grants-2012_09